Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders von Wanders, RJA, Waterham, HR

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Functions and biosynthesis of plasmalogens in health and disease von Brites, Pedro, Waterham, Hans R, Wanders, Ronald J.A

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Prostate Cancer Proliferation Is Affected by the Subcellular Localization of MCT2 and Accompanied by Significant Peroxisomal Alterations von Valença, Isabel, Ferreira, Ana Rita, Correia, Marcelo, Kühl, Sandra, van Roermund, Carlo, Waterham, Hans R., Máximo, Valdemar, Islinger, Markus, Ribeiro, Daniela

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Inherited disorders of cholesterol biosynthesis von Waterham, HR

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ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations von Kemp, Stephan, Pujol, Aurora, Waterham, Hans R., van Geel, Björn M., Boehm, Corinne D., Raymond, Gerald V., Cutting, Garry R., Wanders, Ronald J.A., Moser, Hugo W.

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Mutations in MVK , encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome von Waterham, Hans R, Poll-The, Bwee Tien, Houten, Sander M, Kuis, Wietse, Duran, Marinus, de Koning, Tom J, van Royen-Kerkhof, Annet, Romeijn, Gerrit J, Frenkel, Joost, Dorland, Lambertus, de Barse, Martina M.J, Huijbers, Wim A.R, Rijkers, Ger T, Wanders, Ronald J.A

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Clinical implications of mutation analysis in primary hyperoxaluria type 1 von Van Woerden, Christiaan S., Groothoff, Jaap W., Wijburg, Frits A., Annink, Carla, Wanders, Ronald J.A., Waterham, Hans R.

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Molecular basis of Refsum disease: Sequence variations in Phytanoyl-CoA Hydroxylase (PHYH) and the PTS2 receptor (PEX7) von Jansen, Gerbert A., Waterham, Hans R., Wanders, Ronald J. A.

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Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil : Frequency of the common IVS14+1G>A mutation ca... von VAN KUILENBURG, André B. P, MULLER, Erik W, HAASJES, Janet, MEINSMA, Rutger, ZOETEKOUW, Lida, WATERHAM, Hans R, BAAS, Frank, RICHEL, Dick J, VAN GENNIP, Albert H

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Mutational Spectrum of d-Bifunctional Protein Deficiency and Structure-Based Genotype-Phenotype Analysis von Ferdinandusse, Sacha, Ylianttila, Mari S., Gloerich, Jolein, Koski, M. Kristian, Oostheim, Wendy, Waterham, Hans R., Hiltunen, J. Kalervo, Wanders, Ronald J.A., Glumoff, Tuomo

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Subcellular localization and physiological role of alpha-methylacyl-CoA racemase von Ferdinandusse, S, Denis, S, IJlst, L, Dacremont, G, Waterham, H R, Wanders, R J

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Identification of PEX7 as the Second Gene Involved in Refsum Disease von van den Brink, Daan M., Brites, Pedro, Haasjes, Janet, Wierzbicki, Anthony S., Mitchell, John, Lambert-Hamill, Michelle, de Belleroche, Jacqueline, Jansen, Gerbert A., Waterham, Hans R., Ronald Wanders, J.A.

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Isoprenoid biosynthesis in hereditary periodic fever syndromes and inflammation von Houten, S M, Frenkel, J, Waterham, H R

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Fatty acid metabolism in Saccharomyces cerevisiae von van Roermund, C W T, Waterham, H R, Ijlst, L, Wanders, R J A

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Isolation of the Pichia pastoris glyceraldehyde-3-phosphate dehydrogenase gene and regulation and use of its promoter von Waterham, Hans R, Digan, Mary Ellen, Koutz, Patricia J, Lair, Stephen V, Cregg, James M

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12.2 Mevalonate kinase deficiency: Impaired isoprenoid synthesis induces IL-1beta production via activation of Rac1 von Kuijk, LM, Frenkel, J, Waterham, HR, Koster, J, Coffer, PJ

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Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy von Wanders, Ronald J.A, Ferdinandusse, Sacha, Denis, Simone, Clayton, Peter T, Graham, Andrew, Rees, John E, Allen, John T, McLean, Brendan N, Brown, Ann Y, Vreken, Peter, Waterham, Hans R

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Identification of human PMP34 as a peroxisomal ATP transporter von Visser, W.F, van Roermund, C.W.T, Waterham, H.R, Wanders, R.J.A

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Isolated Mitochondrial Long-Chain Ketoacyl-CoA Thiolase Deficiency Resulting from Mutations in the HADHB Gene von Das, Anibh M, Illsinger, Sabine, Lucke, Thomas, Hartmann, Hans, Ruiter, Jos P.N, Steuerwald, Ulrike, Waterham, Hans R, Duran, Marinus, Wanders, Ronald J.A

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O64 – 1920 Zellweger spectrum manifestations in adulthood von Berendse, K, Engelen, M, Wanders, RJA, Waterham, HR

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